NDC 55111-284
Fluoxetine hydrochloride 90 mg capsule, delayed release pellets
On the label: Dr.Reddy's Laboratories Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Product details
- Generic drug
- Fluoxetine: every company that makes it
- Form
- capsule, delayed release pellets, oral
- Strength
- 90 mg
- Approval
- ANDA ANDA078572
- On the market since
- Mar 24, 2010
- Package NDCs
55111-284-48- Official label
- DailyMed (National Library of Medicine), updated Jun 22, 2026
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